Canonical Allele Identifier: CA421821278

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873063G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903925G>A , CM000663.2:g.173903925G>A	GRCh38
NC_000001.10:g.173873063G>A , CM000663.1:g.173873063G>A	GRCh37
NC_000001.9:g.172139686G>A	NCBI36
NG_012462.1:g.18454C>T , LRG_577:g.18454C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1359C>T MANE Select	ENSP00000356671.3:p.Ile453=
ENST00000367698.3:c.1359C>T	ENSP00000356671.3:p.Ile453=
ENST00000617423.4:c.744C>T	ENSP00000478688.1:p.Ile248=
NM_000488.3:c.1359C>T , LRG_577t1:c.1359C>T	NP_000479.1:p.Ile453=
XM_005245198.2:c.1215C>T	XP_005245255.1:p.Ile405=
NM_001365052.1:c.1215C>T	NP_001351981.1:p.Ile405=
NM_000488.4:c.1359C>T MANE Select	NP_000479.1:p.Ile453=
NM_001365052.2:c.1215C>T	NP_001351981.1:p.Ile405=
NM_001386302.1:c.1482C>T	NP_001373231.1:p.Ile494=
NM_001386303.1:c.1440C>T	NP_001373232.1:p.Ile480=
NM_001386304.1:c.1338C>T	NP_001373233.1:p.Ile446=
NM_001386305.1:c.1302C>T	NP_001373234.1:p.Ile434=
NM_001386306.1:c.1143C>T	NP_001373235.1:p.Ile381=